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PRIMA

LIMACORPORATE SPA · Model 9013.67.270 · UDI-DI 08033390215428

LHX Prescription
4
510(k) clearances
102
Adverse events
1
Recalls
1
Facilities

Description

PRIMA - Trial Tray #S - Insert #S 7° 40 - +0mm

Recalls

DateFirmReason
2010-01-18Stryker SpineStryker Spine received reports of packaging failures during shipping for the Jam Shidi instruments, which may compromise the sterility of the product.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.